Epigenetic Erosion in Adult Stem Cells: Drivers and Passengers of Aging

被引:11
|
作者
Kosan, Christian [1 ]
Heidel, Florian H. [2 ,3 ]
Godmann, Maren [1 ]
Bierhoff, Holger [1 ,2 ]
机构
[1] Friedrich Schiller Univ Jena, Ctr Mol Biomed, Inst Biochem & Biophys, Hans Knoll Str 2, D-07745 Jena, Germany
[2] Fritz Lipmann Inst FLI, Leibniz Inst Aging, Beutenbergstr 11, D-07745 Jena, Germany
[3] Univ Klinikum Jena, Innere Med Hamatol & Onkol 2, D-07747 Jena, Germany
关键词
adult stem cells; spermatogonial stem cells; hematopoietic stem cells; muscle stem cells; self-renewal; differentiation; epigenetic regulation; tissue maintenance; aging; BECKWITH-WIEDEMANN-SYNDROME; MALE GERM-CELLS; DNA METHYLATION; CLONAL HEMATOPOIESIS; GENE-EXPRESSION; DNMT3A MUTATIONS; SELF-RENEWAL; SOMATIC MUTATIONS; SATELLITE CELLS; CHROMATIN;
D O I
10.3390/cells7120237
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In complex organisms, stem cells are key for tissue maintenance and regeneration. Adult stem cells replenish continuously dividing tissues of the epithelial and connective types, whereas in non-growing muscle and nervous tissues, they are mainly activated upon injury or stress. In addition to replacing deteriorated cells, adult stem cells have to prevent their exhaustion by self-renewal. There is mounting evidence that both differentiation and self-renewal are impaired upon aging, leading to tissue degeneration and functional decline. Understanding the molecular pathways that become deregulate in old stem cells is crucial to counteract aging-associated tissue impairment. In this review, we focus on the epigenetic mechanisms governing the transition between quiescent and active states, as well as the decision between self-renewal and differentiation in three different stem cell types, i.e., spermatogonial stem cells, hematopoietic stem cells, and muscle stem cells. We discuss the epigenetic events that channel stem cell fate decisions, how this epigenetic regulation is altered with age, and how this can lead to tissue dysfunction and disease. Finally, we provide short prospects of strategies to preserve stem cell function and thus promote healthy aging.
引用
收藏
页数:19
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